Rasal1 Variant Search Result - Rat Genome Database

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117 records found for search term Rasal1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
21070214	CV789753	single nucleotide variant	NM_001301202.2(RASAL1):c.-64C>T	not provided [RCV000986162]	likely benign	12	113135526	113135526	Human		name
15186163	CV730829	single nucleotide variant	NM_001301202.2(RASAL1):c.2225+7G>A	not provided [RCV000886899]	likely benign	12	113101882	113101882	Human		name
21074331	CV796696	single nucleotide variant	NM_001301202.2(RASAL1):c.1375-9T>G	not provided [RCV000994987]	uncertain significance	12	113108231	113108231	Human		name
598184065	CV3902097	single nucleotide variant	NM_001301202.2(RASAL1):c.12C>G (p.Ser4Arg)	not specified [RCV005265705]	uncertain significance	12	113135451	113135451	Human		name
15102754	CV702138	single nucleotide variant	NM_001301202.2(RASAL1):c.240C>T (p.His80=)	not provided [RCV000959346]	benign	12	113127870	113127870	Human		name
156257163	CV2397847	single nucleotide variant	NM_001301202.2(RASAL1):c.47C>G (p.Ala16Gly)	not specified [RCV004239317]	uncertain significance	12	113135416	113135416	Human		name
401932441	CV2816888	single nucleotide variant	NM_001301202.2(RASAL1):c.534G>A (p.Pro178=)	not provided [RCV003392043]	likely benign	12	113119236	113119236	Human		name
405659646	CV3312275	single nucleotide variant	NM_001301202.2(RASAL1):c.60G>C (p.Lys20Asn)	not specified [RCV004438595]	uncertain significance	12	113135403	113135403	Human		name
15129776	CV753110	single nucleotide variant	NM_001301202.2(RASAL1):c.717C>T (p.Ala239=)	not provided [RCV000919889]	likely benign	12	113117087	113117087	Human		name
15098773	CV753111	single nucleotide variant	NM_001301202.2(RASAL1):c.342A>G (p.Ala114=)	not provided [RCV000914328]	likely benign	12	113121595	113121595	Human		name
21074336	CV796701	single nucleotide variant	NM_001301202.2(RASAL1):c.65T>C (p.Val22Ala)	not provided [RCV000994992]	uncertain significance	12	113135398	113135398	Human		name
155977163	CV2324944	single nucleotide variant	NM_001301202.2(RASAL1):c.214G>T (p.Val72Leu)	not specified [RCV004175200]	uncertain significance	12	113128087	113128087	Human		name
401763089	CV2710436	single nucleotide variant	NM_001301202.2(RASAL1):c.115G>A (p.Val39Met)	not specified [RCV004317590]	uncertain significance	12	113130892	113130892	Human		name
401932440	CV2816887	single nucleotide variant	NM_001301202.2(RASAL1):c.1650G>A (p.Gly550=)	not provided [RCV003392042]	likely benign	12	113107104	113107104	Human		name
405659620	CV3312266	single nucleotide variant	NM_001301202.2(RASAL1):c.200A>G (p.Gln67Arg)	not specified [RCV004438586]	uncertain significance	12	113128101	113128101	Human		name
405659632	CV3312270	single nucleotide variant	NM_001301202.2(RASAL1):c.247A>G (p.Ile83Val)	not specified [RCV004438590]	likely benign	12	113127863	113127863	Human		name
598184040	CV3902093	single nucleotide variant	NM_001301202.2(RASAL1):c.289G>A (p.Asp97Asn)	not specified [RCV005265701]	uncertain significance	12	113127821	113127821	Human		name
598184136	CV3902107	single nucleotide variant	NM_001301202.2(RASAL1):c.287C>G (p.Ala96Gly)	not specified [RCV005265715]	uncertain significance	12	113127823	113127823	Human		name
15166198	CV713346	single nucleotide variant	NM_001301202.2(RASAL1):c.278C>T (p.Ala93Val)	not provided [RCV000971121]	benign	12	113127832	113127832	Human		name
15185139	CV724896	single nucleotide variant	NM_001301202.2(RASAL1):c.2106C>T (p.Ala702=)	not provided [RCV000886614]	benign	12	113102008	113102008	Human		name
15173291	CV724897	single nucleotide variant	NM_001301202.2(RASAL1):c.1092C>T (p.His364=)	not provided [RCV000884006]	benign	12	113114889	113114889	Human		name
15165447	CV753108	single nucleotide variant	NM_001301202.2(RASAL1):c.1495C>T (p.Leu499=)	not provided [RCV000926625]	benign	12	113108102	113108102	Human		name
15098768	CV753109	single nucleotide variant	NM_001301202.2(RASAL1):c.1387C>T (p.Leu463=)	not provided [RCV000914327]	likely benign	12	113108210	113108210	Human		name
21074332	CV796697	single nucleotide variant	NM_001301202.2(RASAL1):c.1356C>T (p.Phe452=)	not provided [RCV000994988]	benign\|likely benign	12	113112104	113112104	Human		name
21074334	CV796699	single nucleotide variant	NM_001301202.2(RASAL1):c.1293G>A (p.Gly431=)	not provided [RCV000994990]	uncertain significance	12	113112167	113112167	Human		name
21074335	CV796700	single nucleotide variant	NM_001301202.2(RASAL1):c.106G>A (p.Asp36Asn)	not provided [RCV000994991]	uncertain significance	12	113130901	113130901	Human		name
152979887	CV1678261	single nucleotide variant	NM_001301202.2(RASAL1):c.982C>T (p.Arg328Trp)	not specified [RCV002246766]	benign	12	113115656	113115656	Human		name
153349573	CV1693604	duplication	NM_001301202.2(RASAL1):c.1912dup (p.Gln638fs)	not provided [RCV002275989]	uncertain significance	12	113104216	113104217	Human		name
155927775	CV2227391	single nucleotide variant	NM_001301202.2(RASAL1):c.934C>A (p.Leu312Ile)	not specified [RCV004092058]	uncertain significance	12	113115704	113115704	Human		name
156341817	CV2268317	single nucleotide variant	NM_001301202.2(RASAL1):c.718G>C (p.Glu240Gln)	not specified [RCV004138605]	uncertain significance	12	113117086	113117086	Human		name
156044291	CV2268513	single nucleotide variant	NM_001301202.2(RASAL1):c.947G>A (p.Arg316Gln)	not specified [RCV004130199]	likely benign	12	113115691	113115691	Human		name
156274123	CV2277886	single nucleotide variant	NM_001301202.2(RASAL1):c.934C>G (p.Leu312Val)	not specified [RCV004147296]	uncertain significance	12	113115704	113115704	Human		name
155964986	CV2286825	single nucleotide variant	NM_001301202.2(RASAL1):c.733G>C (p.Gly245Arg)	not specified [RCV004142627]	likely benign	12	113116050	113116050	Human		name
156270214	CV2290035	single nucleotide variant	NM_001301202.2(RASAL1):c.407G>A (p.Arg136His)	not specified [RCV004152728]	uncertain significance	12	113121530	113121530	Human		name
156107893	CV2304080	single nucleotide variant	NM_001301202.2(RASAL1):c.871G>A (p.Ala291Thr)	not specified [RCV004170123]	uncertain significance	12	113115767	113115767	Human		name
156058328	CV2305240	single nucleotide variant	NM_001301202.2(RASAL1):c.913C>T (p.Leu305Phe)	not specified [RCV004171168]	uncertain significance	12	113115725	113115725	Human		name
156273972	CV2334071	single nucleotide variant	NM_001301202.2(RASAL1):c.721G>A (p.Glu241Lys)	not specified [RCV004183587]	uncertain significance	12	113117083	113117083	Human		name
155970264	CV2338044	single nucleotide variant	NM_001301202.2(RASAL1):c.983G>A (p.Arg328Gln)	not specified [RCV004186084]	uncertain significance	12	113115655	113115655	Human		name
156272880	CV2344049	single nucleotide variant	NM_001301202.2(RASAL1):c.694C>T (p.Arg232Cys)	not specified [RCV004195658]	uncertain significance	12	113117110	113117110	Human		name
156279731	CV2348371	single nucleotide variant	NM_001301202.2(RASAL1):c.506C>A (p.Thr169Asn)	not specified [RCV004193566]	uncertain significance	12	113119366	113119366	Human		name
401721878	CV2710213	single nucleotide variant	NM_001301202.2(RASAL1):c.521A>G (p.Lys174Arg)	not specified [RCV004317114]	uncertain significance	12	113119249	113119249	Human		name
401782382	CV2719789	single nucleotide variant	NM_001301202.2(RASAL1):c.944G>T (p.Gly315Val)	not specified [RCV004329218]	uncertain significance	12	113115694	113115694	Human		name
401738747	CV2721965	single nucleotide variant	NM_001301202.2(RASAL1):c.998G>A (p.Arg333Gln)	not specified [RCV004326460]	uncertain significance	12	113115640	113115640	Human		name
405659635	CV3312271	single nucleotide variant	NM_001301202.2(RASAL1):c.476G>A (p.Arg159His)	not specified [RCV004438591]	uncertain significance	12	113119396	113119396	Human		name
405659636	CV3312272	single nucleotide variant	NM_001301202.2(RASAL1):c.487G>A (p.Gly163Ser)	not specified [RCV004438592]	uncertain significance	12	113119385	113119385	Human		name
405659640	CV3312273	single nucleotide variant	NM_001301202.2(RASAL1):c.504G>T (p.Glu168Asp)	not specified [RCV004438593]	uncertain significance	12	113119368	113119368	Human		name
405659643	CV3312274	single nucleotide variant	NM_001301202.2(RASAL1):c.560G>A (p.Arg187Gln)	not specified [RCV004438594]	uncertain significance	12	113119210	113119210	Human		name
405659650	CV3312276	single nucleotide variant	NM_001301202.2(RASAL1):c.671A>G (p.Gln224Arg)	not specified [RCV004438596]	uncertain significance	12	113117133	113117133	Human		name
405659652	CV3312277	single nucleotide variant	NM_001301202.2(RASAL1):c.961C>A (p.Arg321Ser)	not specified [RCV004438597]	uncertain significance	12	113115677	113115677	Human		name
405659655	CV3312278	single nucleotide variant	NM_001301202.2(RASAL1):c.985C>T (p.Arg329Cys)	not specified [RCV004438598]	uncertain significance	12	113115653	113115653	Human		name
597783800	CV3593006	single nucleotide variant	NM_001301202.2(RASAL1):c.695G>A (p.Arg232His)	not specified [RCV004854328]	uncertain significance	12	113117109	113117109	Human		name
597706098	CV3593007	single nucleotide variant	NM_001301202.2(RASAL1):c.406C>A (p.Arg136Ser)	not specified [RCV004860469]	uncertain significance	12	113121531	113121531	Human		name
597783810	CV3593009	single nucleotide variant	NM_001301202.2(RASAL1):c.854A>G (p.Asp285Gly)	not specified [RCV004854330]	uncertain significance	12	113115784	113115784	Human		name
597783814	CV3593010	single nucleotide variant	NM_001301202.2(RASAL1):c.718G>A (p.Glu240Lys)	not specified [RCV004854331]	uncertain significance	12	113117086	113117086	Human		name
597706136	CV3593015	single nucleotide variant	NM_001301202.2(RASAL1):c.526C>T (p.Arg176Cys)	not specified [RCV004860473]	uncertain significance	12	113119244	113119244	Human		name
597783827	CV3593018	single nucleotide variant	NM_001301202.2(RASAL1):c.574G>C (p.Ala192Pro)	not specified [RCV004854334]	uncertain significance	12	113119196	113119196	Human		name
598184078	CV3902099	single nucleotide variant	NM_001301202.2(RASAL1):c.980C>G (p.Thr327Ser)	not specified [RCV005265707]	uncertain significance	12	113115658	113115658	Human		name
598184084	CV3902100	single nucleotide variant	NM_001301202.2(RASAL1):c.624G>T (p.Lys208Asn)	not specified [RCV005265708]	uncertain significance	12	113119146	113119146	Human		name
598184115	CV3902104	single nucleotide variant	NM_001301202.2(RASAL1):c.377T>C (p.Met126Thr)	not specified [RCV005265712]	uncertain significance	12	113121560	113121560	Human		name
10449924	CV215444	single nucleotide variant	NM_001301202.2(RASAL1):c.1807T>C (p.Phe603Leu)	not provided [RCV000892478]\|not specified [RCV000203124]	benign\|likely benign\|conflicting interpretations of pathogenicity	12	113105737	113105737	Human		name
156149294	CV2200899	single nucleotide variant	NM_001301202.2(RASAL1):c.1306G>A (p.Ala436Thr)	not specified [RCV004081517]	uncertain significance	12	113112154	113112154	Human		name
156400943	CV2213620	single nucleotide variant	NM_001301202.2(RASAL1):c.2323C>T (p.Arg775Cys)	not specified [RCV004089704]	uncertain significance	12	113100024	113100024	Human		name
155933340	CV2228886	single nucleotide variant	NM_001301202.2(RASAL1):c.1301C>T (p.Pro434Leu)	not specified [RCV004095117]	uncertain significance	12	113112159	113112159	Human		name
156059922	CV2239385	single nucleotide variant	NM_001301202.2(RASAL1):c.1901C>T (p.Pro634Leu)	not specified [RCV004114119]	uncertain significance	12	113104228	113104228	Human		name
156278438	CV2252080	single nucleotide variant	NM_001301202.2(RASAL1):c.2045G>C (p.Cys682Ser)	not specified [RCV004122109]	uncertain significance	12	113104005	113104005	Human		name
156311632	CV2260207	single nucleotide variant	NM_001301202.2(RASAL1):c.1357C>G (p.Pro453Ala)	not specified [RCV004120981]	uncertain significance	12	113112103	113112103	Human		name
156154441	CV2266075	single nucleotide variant	NM_001301202.2(RASAL1):c.2288C>T (p.Pro763Leu)	not specified [RCV004126888]	uncertain significance	12	113100059	113100059	Human		name
156196958	CV2293515	single nucleotide variant	NM_001301202.2(RASAL1):c.1470C>G (p.His490Gln)	not specified [RCV004153050]	uncertain significance	12	113108127	113108127	Human		name
156257134	CV2307856	single nucleotide variant	NM_001301202.2(RASAL1):c.2204T>C (p.Leu735Pro)	not specified [RCV004170316]	uncertain significance	12	113101910	113101910	Human		name
156280335	CV2315971	single nucleotide variant	NM_001301202.2(RASAL1):c.2212C>G (p.Arg738Gly)	not specified [RCV004172037]	uncertain significance	12	113101902	113101902	Human		name
156286753	CV2327264	single nucleotide variant	NM_001301202.2(RASAL1):c.2002T>G (p.Leu668Val)	not specified [RCV004174713]	uncertain significance	12	113104048	113104048	Human		name
156055144	CV2343374	single nucleotide variant	NM_001301202.2(RASAL1):c.2090A>G (p.Gln697Arg)	not specified [RCV004197456]	uncertain significance	12	113103960	113103960	Human		name
155984692	CV2344869	single nucleotide variant	NM_001301202.2(RASAL1):c.2107G>A (p.Ala703Thr)	not specified [RCV004191008]	uncertain significance	12	113102007	113102007	Human		name
155927555	CV2349635	single nucleotide variant	NM_001301202.2(RASAL1):c.1367A>C (p.Glu456Ala)	not specified [RCV004204055]	uncertain significance	12	113112093	113112093	Human		name
156192350	CV2356963	single nucleotide variant	NM_001301202.2(RASAL1):c.1810T>A (p.Ser604Thr)	not specified [RCV004204332]	uncertain significance	12	113105734	113105734	Human		name
155929646	CV2389203	single nucleotide variant	NM_001301202.2(RASAL1):c.1738C>A (p.Pro580Thr)	not specified [RCV004235527]	uncertain significance	12	113105806	113105806	Human		name
156061270	CV2391976	single nucleotide variant	NM_001301202.2(RASAL1):c.1792G>A (p.Gly598Arg)	not specified [RCV004235837]	uncertain significance	12	113105752	113105752	Human		name
329396021	CV2463180	single nucleotide variant	NM_001301202.2(RASAL1):c.2110G>C (p.Gly704Arg)	not specified [RCV004274961]	uncertain significance	12	113102004	113102004	Human		name
401723153	CV2674727	single nucleotide variant	NM_001301202.2(RASAL1):c.1631G>A (p.Arg544Gln)	not specified [RCV004294013]	likely benign	12	113107123	113107123	Human		name
401742722	CV2697848	single nucleotide variant	NM_001301202.2(RASAL1):c.2069C>T (p.Ala690Val)	not specified [RCV004300561]	uncertain significance	12	113103981	113103981	Human		name
401747130	CV2698792	single nucleotide variant	NM_001301202.2(RASAL1):c.2212C>T (p.Arg738Trp)	not specified [RCV004301240]	uncertain significance	12	113101902	113101902	Human		name
401759767	CV2701710	single nucleotide variant	NM_001301202.2(RASAL1):c.1631G>C (p.Arg544Pro)	not specified [RCV004314117]	uncertain significance	12	113107123	113107123	Human		name
401737548	CV2718133	single nucleotide variant	NM_001301202.2(RASAL1):c.1744G>A (p.Gly582Ser)	not specified [RCV004315843]	likely benign	12	113105800	113105800	Human		name
401880761	CV2789371	single nucleotide variant	NM_001301202.2(RASAL1):c.1480C>G (p.Gln494Glu)	not specified [RCV004365684]	uncertain significance	12	113108117	113108117	Human		name
404997549	CV2848897	single nucleotide variant	NM_001301202.2(RASAL1):c.1775G>A (p.Arg592His)	Hereditary cancer [RCV003492892]	likely benign	12	113105769	113105769	Human	1	name
405659606	CV3312261	single nucleotide variant	NM_001301202.2(RASAL1):c.1052T>C (p.Met351Thr)	not specified [RCV004438581]	uncertain significance	12	113115216	113115216	Human		name
405659608	CV3312262	single nucleotide variant	NM_001301202.2(RASAL1):c.1447C>G (p.Leu483Val)	not specified [RCV004438582]	uncertain significance	12	113108150	113108150	Human		name
405659612	CV3312263	single nucleotide variant	NM_001301202.2(RASAL1):c.1459C>T (p.Arg487Trp)	not specified [RCV004438583]	uncertain significance	12	113108138	113108138	Human		name
405659615	CV3312264	single nucleotide variant	NM_001301202.2(RASAL1):c.1609C>T (p.Arg537Cys)	not specified [RCV004438584]	uncertain significance	12	113107145	113107145	Human		name
405659617	CV3312265	single nucleotide variant	NM_001301202.2(RASAL1):c.1877T>C (p.Val626Ala)	not specified [RCV004438585]	uncertain significance	12	113104252	113104252	Human		name
405659626	CV3312268	single nucleotide variant	NM_001301202.2(RASAL1):c.2123C>T (p.Thr708Ile)	not specified [RCV004438588]	uncertain significance	12	113101991	113101991	Human		name
405659629	CV3312269	single nucleotide variant	NM_001301202.2(RASAL1):c.2213G>A (p.Arg738Gln)	not specified [RCV004438589]	uncertain significance	12	113101901	113101901	Human		name
407466788	CV3472455	single nucleotide variant	NM_001301202.2(RASAL1):c.2036T>C (p.Leu679Pro)	not specified [RCV004660557]	uncertain significance	12	113104014	113104014	Human		name
407466799	CV3472457	single nucleotide variant	NM_001301202.2(RASAL1):c.1223G>T (p.Arg408Leu)	not specified [RCV004660559]	uncertain significance	12	113112237	113112237	Human		name
407466803	CV3472458	single nucleotide variant	NM_001301202.2(RASAL1):c.1174C>T (p.Arg392Cys)	not specified [RCV004660560]	uncertain significance	12	113114807	113114807	Human		name
407466807	CV3472459	single nucleotide variant	NM_001301202.2(RASAL1):c.1952C>T (p.Thr651Ile)	not specified [RCV004660561]	uncertain significance	12	113104177	113104177	Human		name
407500710	CV3472460	single nucleotide variant	NM_001301202.2(RASAL1):c.1726C>T (p.Arg576Cys)	not specified [RCV004669616]	uncertain significance	12	113105818	113105818	Human		name
597783791	CV3593003	single nucleotide variant	NM_001301202.2(RASAL1):c.2302C>T (p.Arg768Trp)	not specified [RCV004854326]	uncertain significance	12	113100045	113100045	Human		name
597783796	CV3593004	single nucleotide variant	NM_001301202.2(RASAL1):c.1525A>G (p.Ile509Val)	not specified [RCV004854327]	uncertain significance	12	113107229	113107229	Human		name
597783805	CV3593008	single nucleotide variant	NM_001301202.2(RASAL1):c.1460G>A (p.Arg487Gln)	not specified [RCV004854329]	uncertain significance	12	113108137	113108137	Human		name
597706107	CV3593011	single nucleotide variant	NM_001301202.2(RASAL1):c.1441C>A (p.Pro481Thr)	not specified [RCV004860470]	uncertain significance	12	113108156	113108156	Human		name
597706114	CV3593012	single nucleotide variant	NM_001301202.2(RASAL1):c.1288G>A (p.Val430Met)	not specified [RCV004860471]	uncertain significance	12	113112172	113112172	Human		name
597783819	CV3593013	single nucleotide variant	NM_001301202.2(RASAL1):c.1712G>A (p.Gly571Asp)	not specified [RCV004854332]	uncertain significance	12	113105832	113105832	Human		name
597706125	CV3593014	single nucleotide variant	NM_001301202.2(RASAL1):c.1556G>T (p.Gly519Val)	not specified [RCV004860472]	uncertain significance	12	113107198	113107198	Human		name
597783823	CV3593017	single nucleotide variant	NM_001301202.2(RASAL1):c.1396A>G (p.Ser466Gly)	not specified [RCV004854333]	uncertain significance	12	113108201	113108201	Human		name
597783832	CV3593019	single nucleotide variant	NM_001301202.2(RASAL1):c.1267G>T (p.Val423Leu)	not specified [RCV004854335]	uncertain significance	12	113112193	113112193	Human		name
598184047	CV3902094	single nucleotide variant	NM_001301202.2(RASAL1):c.2366A>C (p.Glu789Ala)	not specified [RCV005265702]	uncertain significance	12	113099981	113099981	Human		name
598184052	CV3902095	single nucleotide variant	NM_001301202.2(RASAL1):c.2009A>C (p.Lys670Thr)	not specified [RCV005265703]	uncertain significance	12	113104041	113104041	Human		name
598184057	CV3902096	single nucleotide variant	NM_001301202.2(RASAL1):c.1780G>A (p.Val594Ile)	not specified [RCV005265704]	uncertain significance	12	113105764	113105764	Human		name
598184091	CV3902101	single nucleotide variant	NM_001301202.2(RASAL1):c.1603G>A (p.Val535Ile)	not specified [RCV005265709]	likely benign	12	113107151	113107151	Human		name
598184098	CV3902102	single nucleotide variant	NM_001301202.2(RASAL1):c.1048T>C (p.Ser350Pro)	not specified [RCV005265710]	uncertain significance	12	113115220	113115220	Human		name
598184108	CV3902103	single nucleotide variant	NM_001301202.2(RASAL1):c.1261C>G (p.Pro421Ala)	not specified [RCV005265711]	uncertain significance	12	113112199	113112199	Human		name
598184123	CV3902105	single nucleotide variant	NM_001301202.2(RASAL1):c.2266G>A (p.Glu756Lys)	not specified [RCV005265713]	uncertain significance	12	113100640	113100640	Human		name
598184130	CV3902106	single nucleotide variant	NM_001301202.2(RASAL1):c.1861C>G (p.Arg621Gly)	not specified [RCV005265714]	uncertain significance	12	113104268	113104268	Human		name
15129769	CV753107	single nucleotide variant	NM_001301202.2(RASAL1):c.2393C>T (p.Ala798Val)	not provided [RCV000919888]	likely benign	12	113099954	113099954	Human		name
21074333	CV796698	single nucleotide variant	NM_001301202.2(RASAL1):c.1294C>G (p.Arg432Gly)	not specified [RCV004092711]	uncertain significance	12	113112166	113112166	Human		name
8627185	CV82329	single nucleotide variant	NM_001301202.2(RASAL1):c.2353C>T (p.Arg785Cys)	not specified [RCV004219011]	uncertain significance\|not provided	12	113099994	113099994	Human		name

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